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[ CAS No. 343788-69-2 ] {[proInfo.proName]}

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Chemical Structure| 343788-69-2
Chemical Structure| 343788-69-2
Structure of 343788-69-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 343788-69-2 ]

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Product Details of [ 343788-69-2 ]

CAS No. :343788-69-2 MDL No. :MFCD03265497
Formula : C11H22N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :DMBKWEHXTOCLTC-UHFFFAOYSA-N
M.W : 214.31 Pubchem ID :11310432
Synonyms :

Calculated chemistry of [ 343788-69-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 64.15
TPSA : 55.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.69
Log Po/w (XLOGP3) : 0.91
Log Po/w (WLOGP) : 1.35
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : 0.8
Consensus Log Po/w : 1.38

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.54
Solubility : 6.12 mg/ml ; 0.0286 mol/l
Class : Very soluble
Log S (Ali) : -1.66
Solubility : 4.66 mg/ml ; 0.0218 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.53
Solubility : 6.35 mg/ml ; 0.0296 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.22

Safety of [ 343788-69-2 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 343788-69-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 343788-69-2 ]

[ 343788-69-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 372120-55-3 ]
  • [ 343788-69-2 ]
  • t-butyl 4-((3-bromo-4-(trifluoromethyl)benzyl)amino)-4-methylpiperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
67% j00219J A vial was charged with DCE (10 mL), <strong>[372120-55-3]3-bromo-4-(trifluoromethyl)benzaldehyde</strong> (252 mg, 1.00 mmol, 1.00 equiv), t-butyl 4-amino-4-methylpiperidine-1-carboxylate (214 mg, 1.00 mmol,1.00 equiv), and triethylamine (303 mg, 2.99 mmol, 3.00 equiv). The resulting solution was stirred for 1 h at room temperature, then sodium triacetoxyborohydride (636 mg, 3.00 mmol, 3.00 equiv) was added. The mixture was stirred overnight at room temperature and quenched with water (10 mL), as described in Example 1, Step 6. The residue was chromatographed on a silica gel column to provide 300 mg (67% yield) of t-butyl 4-((3-bromo-4-(trifluoromethyl)benzyl)amino)-4- methylpiperidine-1-carboxylate as a yellow oil. LCMS (ESI, m/z): 451 [M+H].
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